Allegra Allergy
- Product NDC
- 52904-190
- 11-digit product format
- 529040190
- Labeler code
- 52904
- Product ID
- 52904-190_c878ce1e-8153-4871-961b-33c8891dcd27
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Select Corporation
- Application
- NDA020872
- Marketing category
- NDA
- Marketing start
- 2021-12-08
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52904-190-03 | Allegra Allergy | 1 in 1 POUCH | TABLET, FILM COATED | 1 | | 1 |
| 52904-190-03 | Allegra Allergy | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52904-190 | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET, FILM COATED [SELECT CORPORATION] | 1 | Legacy NDC, 2 package rows | 20220415_78d2742f-250a-4c5c-846f-b45078126281.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52904-190-03 | 52904019003 | 1 POUCH in 1 BLISTER PACK (52904-190-03) > 1 TABLET, FILM COATED in 1 POUCH | 1 pouch | 2021-12-08 | 0000-00-00 | No | No | Current |